{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,27]],"date-time":"2026-10-27T11:35:03Z","timestamp":1793100903643,"version":"4.5.0"},"reference-count":32,"publisher":"International Union of Crystallography (IUCr)","issue":"10","license":[{"start":{"date-parts":[[2026,9,3]],"date-time":"2026-09-03T00:00:00Z","timestamp":1788393600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"},{"start":{"date-parts":[[2026,9,3]],"date-time":"2026-09-03T00:00:00Z","timestamp":1788393600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"}],"content-domain":{"domain":["iucr.org","wiley.com","iucrj.org"],"crossmark-restriction":true},"short-container-title":["Acta Crystallogr E Cryst Commun","Acta Cryst E","Acta Cryst Sect E","Acta Crystallogr E","Acta Crystallogr Sect E","Acta Cryst E Cryst Commun","Acta Cryst Sect E Cryst Commun"],"accepted":{"date-parts":[[2026,8,25]]},"published-print":{"date-parts":[[2026,10,1]]},"abstract":"<jats:p>\n                    The title thiophene-chalcone derivative, C\n                    <jats:sub>22<\/jats:sub>\n                    H\n                    <jats:sub>17<\/jats:sub>\n                    ClN\n                    <jats:sub>2<\/jats:sub>\n                    O\n                    <jats:sub>2<\/jats:sub>\n                    S\n                    <jats:sub>2<\/jats:sub>\n                    , contains a planar oxadiazole, a thiophene and two phenyl rings. The dihedral angle between the oxadiazole and thiophene rings is 27.45\u2005(10)\u00b0, and they are oriented with respect to the chlorophenyl and methylphenyl rings at 22.61\u2005(10), 67.07\u2005(8) and 49.16\u2005(10), 87.22\u2005(8)\u00b0, respectively, while the phenyl rings are oriented at 51.78\u2005(9)\u00b0. In the crystal, \u03c0\u2013\u03c0 stacking interactions and C\u2014H...\u03c0(ring) interactions help to consolidate the packing. Hirshfeld surface analysis revealed that the most important contributions to the crystal packing are from H...H (31.6%), H...C\/C...H (20.0%), H...S\/S...H (14.2%) and H...O\/O...H (9.5%) interactions.\n                  <\/jats:p>","DOI":"10.1107\/s2056989026008819","type":"journal-article","created":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T14:35:12Z","timestamp":1787841312000},"page":"1107-1111","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":0,"title":["Synthesis, crystal structure and Hirshfeld surface analysis of 3-[5-(4-chlorophenyl)-2-sulfanylidene-1,3,4-oxadiazol-3-yl]-3-(4-methylphenyl)-1-(thiophen-2-yl)propan-1-one"],"prefix":"10.1107","volume":"82","author":[{"given":"Shailakshi","family":"Jain","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/029zfa075","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sharatha","family":"Kumar","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/029zfa075","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8602-4382","authenticated-orcid":true,"given":"Tuncer","family":"H\u00f6kelek","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"329","published-online":{"date-parts":[[2026,9,3]]},"reference":[{"key":"yz2084_bb1","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1107\/S2056989016000992","volume":"72","author":"Al-Alshaikh","year":"2016","journal-title":"Acta Cryst. 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